Your session is about to expire
← Back to Search
Behavioral Intervention
Diabetes Telecoaching for Type 2 Diabetes
N/A
Recruiting
Research Sponsored by University of Alabama at Birmingham
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Diagnosis of Type 2 Diabetes Mellitus
Living with a permanent physical disability such as spinal cord injury (SCI), spina bifida, multiple sclerosis, stroke, etc.
Must not have
Severe peripheral neuropathy
Severe untreated depression in the past six months
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 48 weeks
Awards & highlights
No Placebo-Only Group
Summary
This trialaims to create an AI-based program to help people with disabilities better manage diabetes with personalized lifestyle changes. #diabetes #AI
Who is the study for?
This trial is for people with Type 2 Diabetes who also have a permanent physical disability like spinal cord injury or multiple sclerosis. Participants must be able to speak and read English but can't join if they've had severe heart issues, kidney failure, untreated depression recently, are in another diabetes study, don't have a smartphone, or have uncontrolled blood pressure.
What is being tested?
The study is testing an AI-assisted program called AI4DM designed to help individuals with disabilities manage their diabetes through lifestyle changes. It's compared against standard attention-control methods to see how effective it is at controlling blood sugar levels.
What are the potential side effects?
Since this trial involves a telecoaching self-management program rather than medication, traditional side effects aren't expected. However, participants may experience stress or frustration if they find the technology challenging.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have been diagnosed with Type 2 Diabetes.
Select...
I live with a permanent physical disability like SCI or MS.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have severe nerve pain or numbness in my hands or feet.
Select...
I have not had severe untreated depression in the last 6 months.
Select...
I have not had a major heart event in the last year.
Select...
My blood pressure is not well-controlled.
Select...
I have kidney failure.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 48 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~48 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Glycemic Management
Secondary study objectives
Diabetes Quality of life
Dietary intake
Family Support
+7 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: AI4DM Intervention GroupExperimental Treatment1 Intervention
Group II: Attention-control GroupActive Control1 Intervention
Find a Location
Who is running the clinical trial?
University of Alabama at BirminghamLead Sponsor
1,656 Previous Clinical Trials
2,444,285 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have been diagnosed with Type 2 Diabetes.You do not have a smartphone.Your heart beats too fast when you are resting.I have severe nerve pain or numbness in my hands or feet.I have not had severe untreated depression in the last 6 months.I have not had a major heart event in the last year.You are currently participating in any program or treatment related to diabetes.I live with a permanent physical disability like SCI or MS.My blood pressure is not well-controlled.I have kidney failure.
Research Study Groups:
This trial has the following groups:- Group 1: AI4DM Intervention Group
- Group 2: Attention-control Group
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.